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Pteropods are excellent recorders of surface temperature and carbonate ion concentration

  • Scientific Reports 7, Article number: 12645 (2017)
  • doi:10.1038/s41598-017-11708-w
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Abstract

Pteropods are among the first responders to ocean acidification and warming, but have not yet been widely explored as carriers of marine paleoenvironmental signals. In order to characterize the stable isotopic composition of aragonitic pteropod shells and their variation in response to climate change parameters, such as seawater temperature, pteropod shells (Heliconoides inflatus) were collected along a latitudinal transect in the Atlantic Ocean (31° N to 38° S). Comparison of shell oxygen isotopic composition to depth changes in the calculated aragonite equilibrium oxygen isotope values implies shallow calcification depths for H. inflatus (75 m). This species is therefore a good potential proxy carrier for past variations in surface ocean properties. Furthermore, we identified pteropod shells to be excellent recorders of climate change, as carbonate ion concentration and temperature in the upper water column have dominant influences on pteropod shell carbon and oxygen isotopic composition. These results, in combination with a broad distribution and high abundance, make the pteropod species studied here, H. inflatus, a promising new proxy carrier in paleoceanography.

Introduction

Assessing the future impact of ocean acidification, the decline in oceanic pH due to anthropogenic CO2 emissions, on marine ecosystems is difficult, as the complexity of ecosystems cannot be easily replicated in laboratory experiments. However, long-term evidence for ocean acidification and the associated responses of marine calcifiers can be found in the geological record, as past ocean temperature and chemistry can be derived from fossil calcium carbonate shells, as well as ecosystem responses such as species richness and net calcification. One prominent and straightforward candidate for such an approximation (proxy) of past conditions is the oxygen isotopic composition (δ18O), which reflects ocean temperature1. It has been demonstrated in inorganic precipitation studies as well as in direct measurements of biogenically produced calcium carbonate2,3, that the calcium carbonate- water oxygen isotopic equilibrium is determined by temperature and (sea)water δ18O (δ18OSW; see Table 1 for notations). This observation applies to both calcite4,5 and aragonite3,6, with an aragonite-calcite fractionation on the order of 0.7 to 0.9‰7. Most studies have analyzed the calcite produced by foraminifera in this context. Similar to foraminifera, pteropods secrete aragonite close to the calcium carbonate- seawater δ18O equilibrium6,8, making them ideal candidates to study their oxygen isotopic composition. Pteropods are marine holoplanktonic gastropods inhabiting epipelagic and mesopelagic waters, down to >1000 m depths9. Although pteropods are rarely explored as possible oceanographic proxy carriers compared to foraminifera, several aspects of their biology make them interesting targets. The approximately one year life cycle and diel vertical migrations of pteropods may yield a more integrative proxy record across epipelagic and mesopelagic water masses and across seasons in comparison to foraminifera, which are characterized by a shorter life span and potentially shallower calcification depths. Calcification depths of recent pteropods can be estimated by comparing the oxygen isotopic composition to the theoretical δ18O of aragonite precipitated in equilibrium with the seawater (δ18Oara), which is calculated from temperature profiles and δ18OSW. Temperature at the time of calcification can be reconstructed directly from δ18Optero, the oxygen isotopic composition of pteropod shells (recent or fossil).

Table 1: Notations.

δ13C in calcium carbonate shells is assumed to be in equilibrium with, or offset by a constant amount from δ13CDIC, the carbon isotopic composition of dissolved inorganic carbon (DIC; the sum of CO2(aq), H2CO3, HCO3 and CO32−). However, several studies found discrepancies for other groups of calcifiers, e.g. foraminifera10, as physiological processes, such as the respiration of symbionts in foraminifera, influence shell δ13C11. Juranek and colleagues12 found a correlation between pteropod δ13Cptero and carbonate ion concentration and hypothesized that this was caused either by a carbonate ion dependence, also demonstrated for foraminifera13, or by the influence of temperature on metabolic CO2 incorporation.

The life cycle of the pteropod species Heliconoides inflatus (d’Orbigny, 183414), formerly and more commonly known as Limacina inflata, has been estimated to be approximately 7–9 months, with a maximum life span of about one year15,16. Reproduction occurs continuously throughout the year, with females retaining developing embryos in the mantle cavity up to a size of about 70 μm until release of the veliger larvae15. Sediment trap studies revealed high interannual variability in the abundance of H. inflatus as well as a pronounced seasonal cycle in abundance, e.g. in the Sargasso Sea16. Here, the highest flux of shells was found during summer, whereas the flux throughout the rest of the year was very low16,17. While H. inflatus has been found as deep as 1000 m, this species primarily occurs in the upper water column12. Seasonal shifts in pteropod depth habitat were also reported for the Sargasso Sea, with H. inflatus preferring shallower waters in the fall (100 to 250 m) than in the spring/ early summer (200–400 m)9. Diel vertical migration, common in pteropods, has been described for H. inflatus, with most of the population below 200 m during the day and highest night-time abundance in the upper 75m9. The species also undergoes ontogenetic migration: juveniles tend to stay in surface waters, whereas adults are mainly found in deeper waters17.

Here we present δ18Optero and δ13Cptero measurements of Heliconoides inflatus shells to assess the potential of pteropods to serve as proxies of seawater temperature (via δ18O) and carbonate ion concentration (via δ13C). We particularly focus on the calcification depth of the species and characterize environmental controls on shell composition. Our material was collected along a meridional transect in the Atlantic Ocean, ranging from 31° N to 38° S. This provides an unique opportunity to assess calcification depths across the entire Atlantic basin, in contrast to previous sediment trap studies that were conducted within a single oceanographic context12,16,18,19. Furthermore, the broad spatial scope of the study allows us to assess different environmental parameters as controls on the stable isotopic composition in pteropod shells, as oceanographic conditions change significantly over such a large latitudinal range. The calibrations established here will be of use to the ocean acidification and paleo-oceanographic community, as the studied species, H. inflatus, occurs in high abundance in sediments worldwide20, for instance, in the Central and South Atlantic21 or the Caribbean Sea22.

Results

Surface distribution of oceanographic parameters

The warmest surface temperatures in the study area of the Atlantic Ocean, up to ~30 °C, usually occurred in October/November just north of the equator (around 10° N; Fig. 1a). Temperature decreased gradually both north and south of this maximum to approximately 12 °C at 40° S, where our southernmost station (station 66) was located. The surface salinity distribution mimicked this general latitudinal zonation (Fig. 1b), however, at the latitude of the temperature maximum, low salinities of 35 to 36 prevailed. Highest surface salinities (37–37.5) occurred in two locations west of 30° W: one in the North Atlantic at around 25° N and one in the South Atlantic at around 20° S. The three southernmost stations (stations 60, 62, 66) lie in an area characterized by mean salinities between 35 and 36. Theoretical values for δ18O of aragonite (δ18Oara), taking into account δ18O estimates of seawater and ambient temperatures, as well as values for δ13CDIC were calculated for surface waters (Fig. 1c, d; see Methods and Table 1 for notations). The strong influence of temperature on the surface distribution of δ18Oara is evident from the latitudinal zonation of this parameter (Fig. 1c). Lowest surface δ18Oara values (~−1.5‰) occurred just north of the equator at 10° N, in the same area where temperature was highest and salinity lowest. From this minimum, surface δ18Oara increased continuously to the north and to the south until highest values were reached in the southernmost part of the transect (stations 62 and 66: ~+2‰). The distribution of δ13CDIC in surface waters also exhibited latitudinal zonation, with highest values (~+2‰) occurring at the equator around 0° W and in the Western Atlantic south of 40° S (Fig. 1d). From the equator, surface values gradually decreased towards both the north and south with lowest surface δ13CDIC values in the North Eastern Atlantic.

Figure 1
Figure 1

Distribution plots of hydrographic parameters in surface waters in the Atlantic Ocean. (a) temperature (° Celsius), (b) salinity, (c) δ18Oara, and (d) δ13CDIC. Only stations from which pteropods were sampled for this study are shown. Data for panels (a), (b) and (c) are derived from the World Ocean Database38, data for panel (d) are from GLODAP39. The software Ocean Data View (v. 4.6.3, http://odv.awi.de) was used to generate these maps40.

δ18O in the water column and in pteropod shells

Latitudinal variations in calculated δ18Oara for equilibrium aragonite values at different depths in the watercolumn reflect strong thermal stratification between 20° N and 20° S, with a maximum in stratification around the equator (4° N), where values ranged from about −1.1‰ at the surface to +2.6‰ at 300 m depth (Fig. 2a). In comparison, δ18Oara in the southern temperate region, e.g. at 34° S (station 62), was less variable across the water column (from +2.1‰ at the surface to +1.5‰ at 300 m depth).

Figure 2
Figure 2

Latitudinal record of δ18Optero and δ13Cptero in shells of Heliconoides inflatus pteropods. (a) δ18Optero (inversed y-scale) and (b) δ13Cptero along a meridional transect in the Atlantic Ocean. Measurements on individual shells are shown (open circles) and closed circles represent averaged values. δ18Oara and δ13CDIC isopleths for different depths in the watercolumn are shown by colored lines as indicated by the legend.

Individual pteropod δ18Optero values varied with latitude (see Table 2, S2 and Fig. 2a): the lowest values (minimum: −0.44‰) occurred at the equator and increased towards higher latitudes (maximum: +2.11‰). Variability between specimens at each station was close to instrument precision, with an average standard deviation of 0.14 (range 0.05–0.28‰). The pteropod oxygen isotopic composition measured here was comparable to the study of Juranek and coworkers12 on the same species (+0.15 to +2.04‰), in which specimens from a one year-sediment trap in the Sargasso Sea were analyzed. Another study, however, reported more depleted oxygen isotopic values (approximately by 0.8‰)16 for the same species from the Sargasso Sea, which likely derived from low temperature ashing of the samples before isotopic measurement12.

Table 2: Average δ18Optero and δ13Cptero (in ‰) based on measurements of individual pteropod shells (N = number of shells measured; SD = Standard Deviation, n.a. = not available, as n=2).

Average pteropod δ18Optero values were similar to those calculated near the 75m-depth isopleth of δ18Oara (Fig. 2a), with individual measurements corresponding to values typically found between the surface and a maximum depth of 150 m. This result was also illustrated by the strong positive relationship between pteropod δ18Optero and δ18Oara in the upper 75 m of the water column (p < 0.05; R2 = 0.89 to 0.91; Table 3, top). Likewise, we found a strong linear relationship between temperature and pteropod δ18Optero (p < 0.05; R2 = 0.87 to 0.86) in the upper 75 m of the water column (Fig. 3, Table 3, top). δ18Optero also showed a positive, but weaker relationship to carbonate ion concentration (p < 0.05, R2 = 0.64) at the surface, while no statistically significant correlation with salinity was found.

Table 3: Linear relationships between average pteropod shell δ18Optero (top), δ13Cptero (middle and bottom) and water parameters: carbonate ion concentration (μmol/kg), temperature (° Celsius), salinity, Chlorophyll a (Chl a ), δ18Oara (‰) and δ13CDIC (‰). Regressions were performed against parameters at specific depths; the adjusted R2 is reported when p < 0.05. n.s. indicates non-significant linear regressions (p > 0.05). Linear regressions for correlations with water parameters at 50 m depths are listed above the tables, values in parentheses are the respective standard errors.
Figure 3
Figure 3

δ18Optero versus temperature at 50 m depth. We observed a significant negative relationship between δ18Optero and temperature (p < 0.05; R2 = 0.86): δ18Optero  = −0.140 (±0.018) * Temperature + 3.919 (±0.404). Values in brackets indicate the standard error. Average standard deviation is depicted by the error bar in the lower left corner.

δ13C in the water column and in pteropod shells

Pteropod shell δ13Cptero showed little variation in samples that were collected between 32° N and 26° S (+0.77‰ ± 0.23‰), however, δ13Cptero increased sharply with mean values of +1.28, +1.60, and +1.97‰ at the southernmost stations 60, 62, and 66, respectively (Fig. 2b, Table 2 and S2). Calculated variation of δ13CDIC in the water column was highest at low latitudes, where the variability of δ13Cptero in pteropod shells was very low (Fig. 2b). Pteropod shell δ13Cptero at most stations was lower than calculated δ13CDIC in the water column. This result was previously observed in pteropod shells that calcified in shallow waters12, and was attributed to the carbonate ion effect, where higher carbonate ion concentrations caused lower δ13Cptero values than in equilibrium with δ13CDIC (see Discussion). We find the strongest linear relationship between pteropod δ13Cptero and carbonate ion concentration in the upper water column (Fig. 4a), with a negative regression of δ13Cptero = −0.02 * Carbonate (50 m) + 5.31 (p < 0.05, R2 = 0.92; Table 3, middle). Furthermore, we observe linear relationships between pteropod δ13Cptero and temperature and salinity, but none with δ13CDIC (Table 3, middle). Pteropod shells from the southernmost stations have high δ13Cptero values, where phytoplankton standing stock was high in surface waters (see Discussion below and Fig. 4b). We observe a significant positive relationship between δ13Cptero and δ18Optero in pteropod shells (p < 0.05, R2 = 0.68; Fig. 5). Interestingly, this relationship is mostly influenced by measurements performed on shells from the three southernmost stations (60, 62 & 66; indicated by open circles in Fig. 5): omitting these stations renders the relationship statistically non-significant (p > 0.05). Comparison of our results to previous findings on the same species16,18,19 revealed that the slope was similar to prior work (Fig. 5). However, the δ13Cptero values presented here cover a broader range than observed in previous studies that were located in environments with less oceanographic variation (e.g., sediment trap studies, Sargasso Sea).

Figure 4
Figure 4

Relationship between δ13Cptero and water parameters. (a) δ13Cptero versus average carbonate ion concentration in the upper 80 m. The carbonate ion effect on δ13Cptero is seen in the negative relationship between carbonate ion concentration and δ13Cptero (solid line). Due to high phytoplankton productivity related 13C enrichment, stations 60, 62 & 66 were removed; the horizontal line indicates the application limit of the calibration (see text). (b) δ13Cptero versus chlorophyll a (Chl. a) fluorescence. Stations 60, 62 & 66 marked in red and station 60 is marked by an asterisk (see Discussion). Error bars in the lower left corner indicate average standard deviation.

Figure 5
Figure 5

Linear relationships between pteropod shell δ13Cptero and δ18Optero. Our data: δ13Cptero = 0.54 * δ18Optero + 0.50 with p = 0.001078 and R2 = 0.68, as denoted by the black line. Grey lines indicate relationships found for the same species by other researchers: dashed (R2 = 0.3, Sargasso Sea)16, dot-dashed (R2 = 0.2, Cape Blanc)19, dotted (R2 = 0.5, Cape Blanc)18. Small black filled circles denote our measurements (triplicates, station 50 in duplicates) from all stations, with measurements from the three southernmost stations (60, 62, 66) depicted in red. The cross in the lower right corner indicates standard deviation (for δ13Cptero and δ18Optero).

Discussion

Deriving past ocean temperature and chemistry from fossil pteropod shells provides a wealth of information about past climate change events. The present study shows that the species H. inflatus is well suited for paleo-reconstructions, as the stable isotopic composition of their shells can be used to track two climate change indicators: δ18Optero records temperature (Fig. 3) and carbonate ion concentration is traced by δ13Cptero (Fig. 4a). Both proxies can be measured simultaneously on a single pteropod shell, making pteropods particularly promising new proxy carriers. Furthermore, we demonstrate that H. inflatus records latitudinal ranges of surface water parameters, as suggested previously from sediment trap studies at a local scale12,16. We confirm shallow water calcification of this species for a large area of the Atlantic Ocean (31° N to 38° S), which, in combination with its basin-wide distribution, renders H. inflatus an ideal candidate for proxy reconstructions.

Based on a comparison between the oxygen isotopic composition of pteropod shells and that of seawater, we observed no systematic latitudinal variation in calcification depth (Fig. 2a). Oxygen isotopic values for H. inflatus strongly correlated with δ18Oara equilibrium values in the upper 75 m of the water column (Fig. 2a, Table 3, top). These findings corroborate observations from other studies on the same species in the Sargasso Sea, suggesting calcification from 50–250 m depths12,16. Such shallow calcification depths are in contrast to reported preferential occurrences of H. inflatus in deeper waters (to 600 m) in the Sargasso Sea17. One possible explanation is that pteropods preferentially calcify near the surface, where calcification is energetically favored due to warmer temperatures, affecting calcium carbonate saturation. Furthermore, most chlorophyll a, and thus potential food resources, occurs in the upper water column, which may be another reason why H. inflatus calcifies in shallow waters.

Pteropod shells are produced over several months, therefore reflecting the sum of environmental conditions experienced throughout the animal’s life. Thus, single-shell measurements, as presented here, are an average of these conditions, with a bias toward the more recently calcified material, as this makes up the largest part of the shell16. Pteropods alter their depth habitat daily, seasonally, and ontogenetically9,17. Consequently, the aragonite of a single pteropod shell could have been produced across a range of depths. Accordingly, the estimated calcification depth of about 75 m may be the average of varying isotopic signatures from different calcification depths. However, several observations argue against this. First, we found no correlation of δ18Optero and temperature below 100 m. Second, other studies on the same species also found that H. inflatus mostly calcified in the upper water column, rather than in deeper waters12,16. The material of a single pteropod shell is probably also the product of several seasons, as the average life span of several pteropod species is on the order of one year15. Sediment trap material is ideal to study the effect of seasonality on the stable isotopic composition of pteropods. Two other studies12,16 found that δ18Optero measurements on seasonal H. inflatus samples from sediment traps usually correlate strongly with seasonal temperature variations in the water column. The absence of an offset in time between δ18Optero and δ18Oara in these studies indicates that the bulk of the shell must have been precipitated within the few months prior to collection, making pteropods reliable recorders of surface water masses.

Carbon isotopic composition of pteropod shells was relatively invariant along the meridional transect in the Atlantic Ocean, with the exception of higher δ13Cptero values at stations south of 30°S (60, 62 and 66; Fig. 4a). Phytoplankton standing stock (chlorophyll a concentration) was very high in surface waters (upper 75 m of the water column) in the south subtropical convergence province (stations 62 and 66, see ref.23). Photosynthesis actively removes the lighter carbon isotopes from the water column DIC reservoir, resulting in 13CDIC enrichment. Since pteropods use ambient DIC to build their shells, δ13Cptero will also be higher in regions with high rates of photosynthesis, as was observed at these southernmost stations (Fig. 4b). The positive relationship between δ13Cptero and chlorophyll a at 25 and 50 m depth (Table 3, middle, p < 0.05, R2 = 0.80 and 0.73, respectively) also reflects the effect of photosynthesis on δ13Cptero. Additionally, H. inflatus specimens from southern temperate waters (south of 34°S) along a similar transect (AMT24) were reported to be morphologically distinct, having coarser and thicker shells than specimens from the rest of the transect, and thus may represent a distinct population or (sub)species (referred to as H. inflatus S)24. In these respects, station 60 (30.20 °S) should be regarded as a transitional station: it is located in the oligotrophic south Atlantic gyral province with low chlorophyll a concentrations and H. inflatus specimens that were morphologically similar to specimens from tropical and subtropical waters, but average δ13Cptero in their shells was relatively high (Fig. 4b, station marked by asterisk). While the (calcium) isotopic signature of foraminiferal sub-species has been demonstrated to be the same25, small trace element compositional differences can still be caused by depth habitat preferences of different sub-species26. All pteropods analyzed here calcify in the same water depth (upper 75 m, Fig. 2a), allowing us to assume that the potentially different (sub) species have similar isotopic signatures under the same environmental conditions. Pteropod δ13Cptero did not show much variation between 32° N and 26° S (Fig. 2b), where chlorophyll a concentration was much lower (Fig. 4b). Apparently, photosynthesis by these low phytoplankton concentrations did not cause a 13C enrichment of the DIC pool, explaining the relatively low δ13Cptero values of the pteropods across most of the transect (average + 0.70‰). However, as we observe no correlation between chlorophyll a fluorescence and δ13Cptero in the majority of the pteropod shells analyzed (Fig. 4b), other influences on δ13Cptero should be explored, such as the carbonate ion effect. This effect was reported in foraminifera13,27 and in pteropods12, and describes the inverse relationship between carbonate ion concentration and δ13Cptero, which is also apparent in our results (Fig. 4a, R2 = 0.94, p < 0.05). For the southernmost stations, it is impossible to disentangle the effects of 13C enrichment via photosynthesis and the carbonate ion effect on pteropod δ13Cptero (Table 3). We therefore performed linear regressions on δ13Cptero and water column parameters while excluding stations 60, 62, and 66 (Table 3, bottom). Excluding these three stations clearly demonstrates the carbonate ion effect on δ13Cptero (Table 3, bottom, R2 = 0.84, p < 0.05) in the upper water column of an area where no 13C enrichment is occurring (no effect of chlorophyll a on δ13Cptero; Table 3, bottom, p > 0.05).

Our study shows that the pteropod species H. inflatus calcifies across a number of oceanographic provinces in the Atlantic at the same, shallow depth (upper 75 m of the water column, Fig. 2a, Table 3), making these pteropod shells good recorders of surface water masses. Correlations between stable isotopic composition of shells and parameters of the water column indicate that H. inflatus shells are good proxy carriers for temperature and carbonate ion reconstructions with the following regressions (for values at 50 m depth):

t e m p e r a t u r e = δ 18 O p t e r o 3.919 ( ± 0.404 ) 0.140 ( ± 0.140 )
(1)

with p < 0.05, R2 = 0.86 (Table 3, top), and

c a r b o n a t e i o n c o n c e n t r a t i o n = δ 13 C p t e r o 3.067 ( ± 0.386 ) 0.010 ( ± 0.002 )
(2)

with p < 0.05, R2 = 0.92 (Table 3, bottom), only valid for δ13Cptero < 1‰ (see Discussion below).

The uncertainty in the estimations for temperature (equation 1) and carbonate ion concentration (equation 2) based on an error propagation calculation sums to an error of 17% and 25%, respectively, assuming a measurement precision of 0.09‰ and 0.05‰ for the measurements of δ18Optero and δ13Cptero, respectively. Please note that the regressions reported above (equations 1 and 2) have been derived from different datasets. While the δ18Optero-temperature regression (equation 1) includes all stations, the δ13Cptero-carbonate ion regression (equation 2) is not valid for high productivity waters (here 31° S to 38° S), as the δ13Cptero in these regions may be influenced by 13C enrichment (see Discussion above). Consequently, the calibration (equation 2) should only be used on δ13Cptero values < 1‰ limiting the resolvable carbonate ion concentration to values of 200 μmol/kg-sw or higher.

Heliconoides inflatus is a pteropod species that not only occurs in the Atlantic, but has a circumglobal distribution in tropical and subtropical waters (including the Caribbean, Mediterranean and Indo-Pacific). Therefore, it is a good proxy carrier to assess surface water variations over paleo-timescales worldwide. Heliconoides is the oldest known pteropod genus in the fossil record (72–79 million years ago (mya)28), and the species H. inflatus has been described to occur at least since the early Miocene (Aquitanian) from the Aquitaine and North Sea basins (23.03–20.44 mya29 and pers. comm. Janssen 2017). One limitation on the application of this new proxy is the occurrence of well-preserved pteropod shells in sediments, confined to waters above the lysocline of aragonite. However, there are a number of sediment cores available in which H. inflatus is abundant and where the calibrations reported here can be applied. The CAR-MON2 core22 would be an ideal candidate from the Caribbean Sea, as it contains H. inflatus in great abundance. The core spans the last 250,000 years, and the associated changes in the ocean’s temperature and carbonate ion concentration during glacial/ interglacial cycles are well resolvable by the proxy calibrations reported here. This holds true even under the restriction of the δ13Cptero calibration, as surface carbonate ion concentration in the Caribbean Sea has been >250 μmol/kg-sw for the last 100, 000 years30.

Methods

Pteropod collection

Bulk zooplankton was collected on the Atlantic Meridional Transect Cruise 22 (AMT22) between 10/19/2012 and 11/16/2012. Oblique tows were conducted with bongo nets (200 µm, 333 µm), towed between on average 361 m depth and the sea surface. Pteropods were collected from a total of 11 stations, between 31° N to 38° S latitude, in the pre-dawn hours (Table S1). After collection, pteropods were immediately fixed in pure ethanol (96–99%), which was renewed within 12–24 hours of collection. Specimens were stored at −20 °C until analysis.

Measurements of stable isotopes (δ18O and δ13C) of pteropod shells

Pteropods (H. inflatus) within a narrow size range (800–1200 μm shell width) were removed from ethanol and dried at room temperature. All individual shells were weighed on a microbalance to ensure sufficient material for isotopic analysis (sample mass 120 ± 60 (1 SD) μg on average). Shells were broken to allow removal of the soft-tissue. All shell pieces were collected, triple rinsed with ultrapure water, dried at room temperature and weighed. The isotopic composition was analyzed at the Leibniz Laboratory for Radiometric Dating and Stable Isotope Research (Kiel University, Germany) using a Kiel IV carbonate preparation device connected to a ThermoScientific MAT 253 mass spectrometer. The aragonitic shells were reacted with 100% phosphoric acid (H3PO4) under vacuum at 75 °C, and the evolved carbon dioxide gas was analyzed eight times for each individual sample. All values are reported in the Vienna Pee Dee Belemnite notation (VPDB) relative to NBS19. Precision of all different laboratory internal and international standards (NBS19) is ≤±0.05‰ for δ13C and ≤±0.09‰ for δ18O values. For notations related to shell chemistry, see Table 1.

Isotope values are reported in standard δ notation where:

δ 18 O= [ O 18 O 16 sample O 18 O 16 standard 1 ] 1000
(3)
δ 13 C= [ C 13 C 12 sample C 13 C 12 standard 1 ] 1000
(4)

Averaged values of triplicate measurements are reported, except for station 50, where measurements were only possible in duplicate (Tables 2 and S2).

Seawater parameters: temperature, salinity, carbonate chemistry and chlorophyll a

Seawater temperature, salinity, and chlorophyll a concentrations in the upper 500 m of the water column were obtained by conductivity-temperature-depth (CTD) casts (Sea-Bird Electronics, models: ocean logger, SBE45, 9plus) and Chelsea MKIII Aquatracka Fluorometer, respectively. Sensors were calibrated and data archived by the British Oceanographic Data Centre (BODC). Discrete seawater samples taken from Niskin bottles were used to measure pH, TA (total alkalinity) and DIC. In order to calibrate the CTD chlorophyll fluorometer, discrete Chlorophyll a samples were analyzed fluorometrically following standard acetone extraction31. Briefly, discrete chlorophyll a samples were filtered through GF/F filters (0.7 μm) and placed in acetone for 18–36 hours before fluorescence was measured on a Turner Designs AU10 fluorometer.

pH was measured (~11 samples per station) spectrophotometrically according to Clayton and Byrne32. TA was measured at selected depths, including ~3 samples per station (e.g. at approximately 300, 100 and 2 m depth for station 15), and analyzed by open-cell-titration33. TA measurements were related to salinity and temperature34 according to the polynomial described by Lee and colleagues35, and were subsequently used to estimate TA at all depths. TA and pH were used to calculate the complete C-system (DIC, bicarbonate, carbonate, Omega and Revelle Factor at all depths) using the CO2SYS software36. These calculations were consistent with measured DIC (at selected depths, ~3 depths per station, same depths as TA measurements) and surface pCO2 (CO2 partial pressure) measured continuously every 20 minutes34.

Seawater composition in the sampling area

In order to characterize environmental controls on pteropod stable isotopic composition (δ18Optero and δ13Cptero), seawater δ18Oara and δ13CDIC isopleths were calculated (surface to 300 m). The salinity- δ18OSW (seawater: sw) calibrations from Le Grande and Schmidt37 for Atlantic provinces were used, with CTD-derived salinity (S) as an input parameter: North Atlantic (δ18OSW = 0.55*S − 18.98), Tropical Atlantic (δ18OSW = 0.15*S − 4.61) and Southern Atlantic (δ18OSW = 0.51*S −17.40). Thereafter, δ18Oara was calculated from temperature and δ18OSW according to: δ18Oara = (T−20)/(−4.42) + δ18OSW7, using temperature (T) from CTD measurements. There was no suitable calibration for the correlation of δ13CDIC and DIC, therefore we used the GLODAP data set (http://cdiac.ornl.gov/oceans/GLODAPv238) to calculate linear regressions between δ13CDIC and DIC. We defined six oceanic provinces according to latitude (45°N-30°N, 30°N-15°N, 15°N -0°N, 0°S-23°S, 23°S-30°S, 30°S-45°S) and used all available data in the upper 105 m between 10° E and 60° E, yielding six regressions for the relationship between δ13CDIC and DIC (Table S3). The uncertainty in these calculations based on an error propagation calculation assuming a DIC concentration of 2200 (±10) μmol/kg sums to an average error of 22% for the δ13CDIC estimation and to an error of 5% in the δ18OSW estimation, when assuming a salinity of 35 (±0.1) and temperature of 24 (±0.1) ° C. These values have been calculated using the standard errors listed in Table S3 and the respective publications7,37. Data from the World Ocean Database (WOD)38 and GLODAP39 were used to generate surface distribution maps of the Atlantic for temperature, salinity and seawater δ18Oara and δ13CDIC. Plots present average values from October through November in order to obtain a representation of the typical surface distribution of these parameters during the period of the cruise (10/13/2012 to 11/19/2012). The WOD38 data collection contained all surface data available from 1986 to 2011, and the GLODAP39 data collection contained all data from 1972 to 2011.

Statistical analyses

To test the effect of temperature, salinity, carbonate ion concentration, chlorophyll a concentration, δ18Oara and δ13CDIC on pteropod shell isotopic composition (δ18Optero and δ13Cptero), linear regressions were calculated for specific depths (2, 25, 50, 75, 100, 200, 250, 300 m). Temperature, salinity and chlorophyll a were taken from the CTD casts. Carbonate ion concentration was interpolated to these depths, while δ18Oara and δ13CDIC were calculated at these depths (see above).

Data availability

All data generated or analyzed during this study are included in this published article (and its Supplementary Information files).

Additional Information

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References

  1. 1.

    Emiliani, C. Pleistocene temperatures. J. Geol. 63, 538–578 (1955).

  2. 2.

    McCrea, J. M. On the isotopic chemistry of carbonates and a paleotemperature scale. The Journal of Chemical Physics 18, 849–857 (1950).

  3. 3.

    Tarutani, T., Clayton, R. N. & Mayeda, T. K. The effect of polymorphism and magnesium substitution on oxygen isotope fractionation between calcium carbonate and water. Geochimica et Cosmochimica Acta 33, 987–996 (1969).

  4. 4.

    O’Neil, J. R., Clayton, R. N. & Mayeda, T. K. Oxygen isotope fractionation in divalent metal carbonates. J. Chem. Phys. 51, 547–5558 (1969).

  5. 5.

    Kim, S.-T. & O’Neil, J. R. Equilibrium and nonequilibrium oxygen isotope effects in synthetic carbonates. Geochimica et Cosmochimica Acta 61, 3461–3475 (1997).

  6. 6.

    Grossman, E. L. & Ku, T.-L. Oxygen and carbon isotope fractionation in biogenic aragonite: Temperature effects. Chemical Geology: Isotope Geoscience section 59, 59–74 (1986).

  7. 7.

    Böhm, F. et al. Oxygen isotope fractionation in marine aragonite of coralline sponges. Geochimica et Cosmochimica Acta 64, 1695–1703 (2000).

  8. 8.

    Grossman, E. L., Betzer, P. R., Dudley, W. C. & Dunbar, R. B. Stable isotopic variation in pteropods and atlantids from North Pacific sediment traps. Marine Micropaleontology 10, 9–22 (1986).

  9. 9.

    Wormuth, J. H. Vertical distributions and diel migrations of Euthecosomata in the northwest Sargasso Sea. Deep Sea Research Part A. Oceanographic Research Papers 28, 1493–1515 (1981).

  10. 10.

    Deuser, W. G. Seasonal variations in isotopic composition and deep-water fluxes of the tests of perennially abundant planktonic foraminifera of the Sargasso Sea; results from sediment-trap collections and their paleoceanographic significance. The Journal of Foraminiferal Research 17, 14–27 (1987).

  11. 11.

    Spero, H. J. Do planktic foraminifera accurately record shifts in the carbon isotopic composition of seawater ΣCO2? Marine Micropaleontology 19, 275–285 (1992).

  12. 12.

    Juranek, L. W., Russell, A. D. & Spero, H. J. Seasonal oxygen and carbon isotope variability in euthecosomatous pteropods from the Sargasso Sea. Deep Sea Research Part I: Oceanographic Research Papers 50, 231–245 (2003).

  13. 13.

    Spero, H. J., Bijma, J., Lea, D. W. & Bemis, B. E. Effect of seawater carbonate concentration on foraminiferal carbon and oxygen isotopes. Nature 390, 497–500 (1997).

  14. 14.

    d’Orbigny, A. Voyage dans l’Amérique méridionale (le Brésil, la république orientale de l’Uruguay, la république Argentine, la Patagonie, la république du Chili, la république de Bolivia, la république du Pérou), exécuté pendant les années 1826, 1827, 1828, 1829, 1830, 1831, 1832 et 1833. (5. - Paris (Bertrand); Strasbourg (Levrault), 1834–1847).

  15. 15.

    Wells, F. E. Jr. Seasonal patterns of abundance and reproduction of euthecosomatous pteropods off Barbados West Indies. Veliger 18, 241–248 (1976).

  16. 16.

    Fabry, V. J. & Deuser, W. G. Seasonal Changes in the Isotopic Compositions and Sinking Fluxes of Euthecosomatous Pteropod Shells in the Sargasso Sea. Paleoceanography 7, 195–213 (1992).

  17. 17.

    Almogi-Labin, A., Hemleben, C. & Deuser, W. G. Seasonal variation in the flux of euthecosomatous pteropods collected in a deep sediment trap in the Sargasso Sea. Deep Sea Research Part A. Oceanographic Research Papers 35, 441–464 (1988).

  18. 18.

    Fischer, G., Kalberer, M., Donner, B. & Wefer, G. In Use of Proxies in Paleoceanography: Examples from the South Atlantic (eds Gerhard Fischer & Gerold Wefer) 191–206 (Springer Berlin Heidelberg, 1999).

  19. 19.

    Kalberer, M. et al. Seasonal sedimentation and stable isotope records of pteropods off Cap Blanc. Marine Geology 113, 305–320 (1993).

  20. 20.

    Bé, A. W. H. & Gilmer, R. W. In Oceanic Micropaleontology (ed A.T.S. Ramsay) 733–807 (Academic Press, 1977).

  21. 21.

    Gerhardt, S. & Henrich, R. Shell preservation of Limacina inflata (Pteropoda) in surface sediments from the Central and South Atlantic Ocean: a new proxy to determine the aragonite saturation state of water masses. Deep Sea Research Part I: Oceanographic Research Papers 48, 2051–2071 (2001).

  22. 22.

    Wall-Palmer, D. et al. Pteropods from the Caribbean Sea: variations in calcification as an indicator of past ocean carbonate saturation. Biogeosciences 9, 309–315 (2012).

  23. 23.

    Burridge, A. K., Tump, M., Vonk, R., Goetze, E. & Peijnenburg, K. T. C. A. Diversity and distribution of hyperiid amphipods along a latitudinal transect in the Atlantic Ocean. Progress in Oceanography, http://dx.doi.org/10.1016/j.pocean.2016.08.003 (in press).

  24. 24.

    Burridge, A. K. et al. Diversity and abundance of pteropods and heteropods along a latitudinal gradient across the Atlantic Ocean. Progress in Oceanography, https://doi.org/10.1016/j.pocean.2016.10.001 (in press).

  25. 25.

    Hippler, D., Kozdon, R., Darling, K. F., Eisenhauer, A. & Nägler, T. F. Calcium isotopic composition of high-latitude proxy carrier Neogloboquadrina pachyderma (sin.). Biogeosciences 6, 1–14 (2009).

  26. 26.

    Steinke, S. et al. Mg/Ca ratios of two Globigerinoides ruber (white) morphotypes: Implications for reconstructing past tropical/subtropical surface water conditions. Geochemistry, Geophysics, Geosystems 6, Q11005 (2005).

  27. 27.

    Bijma, J., Hemleben, C., Huber, B. T., Erlenkeuser, H. & Kroon, D. Experimental determination of the ontogenetic stable isotope variability in two morphotypes of Globigerinella siphonifera (d’Orbigny). Marine Micropaleontology 35, 141–160 (1998).

  28. 28.

    Janssen, A. W. & Peijnenburg, K. T. C. A. An overview of the fossil record of Pteropoda. Cainozoic Research 17, 3–10 (2017).

  29. 29.

    Cahuzac, B. & Janssen, A. W. Eocene to Miocene pteropods (Gastropoda, Euthecosomata) from the Aquitaine Basin, SW France. Scripta Geologica 141, 1–193 (2010).

  30. 30.

    Foster, G. L. Seawater pH, pCO2 and [CO2−3] variations in the Caribbean Sea over the last 130 kyr: A boron isotope and B/Ca study of planktic foraminifera. Earth and Planetary Science Letters 271, 254–266 (2008).

  31. 31.

    Welschmeyer, N. A. Fluorometric analysis of chlorophyll a in the presence of chlorophyll b and pheopigments. Limnology and Oceanography 39, 1985–1992 (1994).

  32. 32.

    Clayton, T. D. & Byrne, R. H. Spectrophotometric seawater pH measurements: total hydrogen ion concentration scale calibration of m-cresol purple and at-sea results. Deep Sea Research Part I: Oceanographic Research Papers 40, 2115–2129 (1993).

  33. 33.

    Dickson, A. G., Sabine, C. L. & Christion, J. R. Guide to best practices for ocean CO2 measurements. PICES Special Publication 3, 191 (2007).

  34. 34.

    Kitidis, V., Brown, I., Hardman-Mountford, N. & Lefevre, N. Surface ocean carbon dioxide during the Atlantic Meridional Transect (1995–2013); evidence of ocean acidification. Progress in Oceanography, doi:10.1016/j.pocean.2016.1008.1005, doi:10.1016/j.pocean.2016.08.005 (in press).

  35. 35.

    Lee, K. et al. Global relationships of total alkalinity with salinity and temperature in surface waters of the world’s oceans. Geophysical Research Letters 33, L19605 (2006).

  36. 36.

    MS Excel program developed for CO2 system calculations. (US Department of Energy, Oak Ridge, Tennessee, 2006).

  37. 37.

    LeGrande, A. N. & Schmidt, G. A. Global gridded data set of the oxygen isotopic composition in seawater. Geophysical Research Letters 33, L12604 (2006).

  38. 38.

    Boyer, T. P. et al. World Ocean Database 2013, NOAA Atlas NESDIS 72, S. Levitus, Ed., A. Mishonov, Technical Ed.; Silver Spring, MD, 209 pp., http://doi.org/10.7289/V5NZ85MT (2013).

  39. 39.

    Olsen, A. et al. The Global Ocean Data Analysis Project version 2 (GLODAPv2) – an internally consistent data product for the world ocean. Earth Syst. Sci. Data 8, 297–323 (2016).

  40. 40.

    Schlitzer, R. Ocean Data View, v. 4.6.3, http://odv.awi.de (2014).

Download references

Acknowledgements

We thank G. Tarran, A. Rees, R. Thomas and scientists from the AMT programme, as well as the crew of the RRS James Cook, for supporting zooplankton and oceanographic data collections on AMT22. NK was funded by grant CP1407 of the Cluster of Excellence ‘The Future Ocean’ (ExC180), which is funded within the framework of the Excellence Initiative by the Deutsche Forschungsgemeinschaft (DFG) on behalf of the German federal and state governments. NK also received a scholarship from Daimler Benz Stiftung and a Martin fellowship from Naturalis Biodiversity Center. A Netherlands Organisation for Scientific Research (NWO) cruise participation grant and Vidi grant 016.161.351 to KP also partially supported this work. EG and the fieldwork for this study were supported under National Science Foundation (USA) grants OCE-1029478 and OCE-1338959. This study is a contribution to the international IMBER project and was supported by the UK Natural Environment Research Council National Capability funding to Plymouth Marine Laboratory and the National Oceanography Centre, Southampton. This is contribution number 312 of the AMT programme. We acknowledge financial support by Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds. Two anonymous reviewers are thanked for their comments, which significantly improved the manuscript.

Author information

Affiliations

  1. Institute of Geosciences, Christian-Albrechts-Universität zu Kiel, Ludewig-Meyn-Str.10, 24118, Kiel, Germany

    • N. Keul
    •  & R. R. Schneider
  2. Naturalis Biodiversity Center, P.O. Box 9517, 2300 RA, Leiden, The Netherlands

    • K. T. C. A. Peijnenburg
  3. Institute for Biodiversity and Ecosystem Dynamics (IBED), University of Amsterdam, P.O. Box 94248, 1090 GE, Amsterdam, The Netherlands

    • K. T. C. A. Peijnenburg
  4. Leibniz-Labor für Altersbestimmung und Isotopenforschung, Christian-Albrechts-Universität zu Kiel, Max-Eyth-Str.11–13, 24118, Kiel, Germany

    • N. Andersen
  5. Plymouth Marine Laboratory, Plymouth, PL1 3DH, United Kingdom

    • V. Kitidis
  6. Department of Oceanography, University of Hawai’i at Mānoa, 1000 Pope Road, Honolulu, HI, 96822, USA

    • E. Goetze

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Contributions

N.K. and K.T.C.A.P. designed the study, K.T.C.A.P., V.K. and E.G. carried out sampling, N.K. and N.A. analyzed the data and N.K. compiled the manuscript with the help of all co-authors.

Competing Interests

The authors declare that they have no competing interests.

Corresponding author

Correspondence to N. Keul.

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